Recent Advances in the Synthesis of Inorganic Materials Using Environmentally Friendly Media

Deep Eutectic Solvents have gained a lot of attention in the last few years because of their vast applicability in a large number of technological processes, the simplicity of their preparation and their high biocompatibility and harmlessness. One of the fields where DES prove to be particularly valuable is the synthesis and modification of inorganic materials—in particular, nanoparticles. In this field, the inherent structural inhomogeneity of DES results in a marked templating effect, which has led to an increasing number of studies focusing on exploiting these new reaction media to prepare nanomaterials. This review aims to provide a summary of the numerous and most recent achievements made in this area, reporting several examples of the newest mixtures obtained by mixing molecules originating from natural feedstocks, as well as linking them to the more consolidated methods that use “classical” DES, such as reline.


Introduction
According to the general definition currently used (EU 2011), a "nanoparticle" (NP) is a discrete (nano-)object where at least one of its characteristic dimensions falls in the range 1-100 nm. This category thus includes objects with a fixed number of such dimensions, such as nanowires/nanotubes (mono-dimensional, 1D) and nanodiscs/nanoplates (2D), as well as nanometric spherical/globular three-dimensional aggregates. Nanoparticles can be further classified according to their organic/inorganic nature. Dendrimers, lyposomes, and polymeric NPs belong to the former group, whereas fullerenes, quantum dots, and metal/metal oxide NPs to the latter [1,2]. Most importantly, nanomaterials are classified according to their size, shape, and properties, and it is this last feature that has led to the blossoming of nanomaterial research in the last few years. The remarkable properties nanoparticles possess (e.g., optical, magnetic, and electrical) can be exploited in a large number of technology-related fields, ranging from electronics [3,4] to biology and medicine [5,6]. The correlation between size/shape and properties in nanomaterials was thoroughly assessed in several investigations, and it was shown that their properties were dramatically dependent on the shapes, dimensions, and porosities of the synthesized nanoobjects; thus, a detailed control of the synthetic route is needed. The structural differences observed ultimately result in remarkably different performances in real-world applications. Among the factors that can be controlled, the most easily tunable is probably temperature. For instance, in the synthesis of metal oxides by the co-precipitation pathway, the temperature at which the drying/calcination of the hydroxide is carried out can vary widely. Despite its apparent "simplicity", the effect of this variation can be quite relevant, as was found, for instance, in the synthesis of nickel (II) oxide NiO, a prototypical p-type, wide-band-gap semiconductor. NiO nanoparticles prepared at 400 • C are smaller and more porous, while larger structures are obtained at 600 • C; the band gaps associated with the latter are larger and the electrochemical performances worse, especially when these nanoparticles are introduced into screen-printed electrodes (SPEs) and employed as electrochemical sensors for selective assays or in Faradic pseudo-capacitors. Other factors that have been found to influence the intercalation of precursors and the sintering of particles, the latter leading to particles of larger sizes, are the reagents used to prepare the precursor hydroxide Ni(OH) 2 : the use of various combinations of nickel salts and inorganic/organic bases as precipitating agents, and the adoption of surfactant-free hydrothermal synthesis or microwave irradiation (which can lead to different results) [7][8][9][10][11][12].
In a large number of studies aiming to control the shape and dimensions of particles, the use of templating agents has been investigated in more detail. Various types of systems have been employed for this purpose, such as, for instance, boric, citric, and ascorbic acids [13]; cholesteric liquid crystals [14]; and different types of surfactants [15]. Here, the use of dendrimers such as poly(amidoamine) (PAMAM) is noteworthy, as it allowed the production of very small NPs with dimensions as low as 1.4 nm [16]. In this contribution, we focus our attention on a new class of environmentally friendly, inherently inhomogeneous, and highly structured family of liquids, Deep Eutectic Solvents, which can naturally exert a templating effect. The most recent developments in the field will be reviewed and additional references will be provided, thus enlarging the literature coverage of the reviews already published on this subject [17][18][19][20].

Brief Description of Deep Eutectic Solvents
Since the "official" birthday of this family of liquids, which can be traced back to the pivotal paper by Abbott in 2003 [21], a fairly large amount of research has been dedicated to them, especially in the last decade. The key feature of these solvents is their very easy and economic preparation, which involves the simple mixing of at least one hydrogen bond donor (HBD) with at least one hydrogen bond acceptor (HBA). In most cases, this takes place in solid phase and in definite ratios, providing mixtures with remarkably lower melting points than those of their individual components. The sometimes very large decrease seen in the melting temperature, which in the prototypical choline chloride:urea 1:2 system ("Reline") [22] can be more than 100 • C with respect to the ideal value obtainable from thermodynamics arguments [23,24], has led to the term "deep" being used to distinguish DESs from other non-ideal physical systems where similar phenomena are observed-e.g., water-DMSO mixtures. Deep Eutectic Solvents were divided into four main classes in the original classification by Abbott, three of which contain a halide anion and a quaternary ammonium cation as HBA (in most cases, choline chloride), and differ in their type of HBD: metal chloride in class I, hydrated metal chloride in class II, organic molecules (such as urea, glycerol, and carboxylic acids) in class III (which is the most populated), and metal halides and urea (or acetamide/ethylene glycol) in class IV. Recently, a new class was introduced ("type V" [25]), containing only hydrogen-bond donors and acceptors and no ions. Other non-negligible valuable traits of Deep Eutectic Solvents are their high sustainability, especially in the subfamily NaDES (Natural DES), where the precursors are benign compounds generally obtained from natural feedstocks, such as choline chloride and carboxylic acids; these therefore have a low toxicity and high biocompatibility and biodegradability [26][27][28]. Additionally, DESs are characterized by their high conductivities, viscosities, and surface tensions; have a low volatility and flammability; and have highly tunable physiochemical properties, considering the large number of possible combinations of precursor salts [29]. These last features are shared with ionic liquids (ILs), which can be considered as the forefathers of DESs. However, ILs are composed (almost entirely) of ions [30,31], whereas DESs, apart from the type V ones, are mixtures that contain polar molecules and ions. A sketch of the desirable technological properties of DESs is provided in Figure 1. considering the large number of possible combinations of precursor salts [29]. These last features are shared with ionic liquids (ILs), which can be considered as the forefathers of DESs. However, ILs are composed (almost entirely) of ions [30,31], whereas DESs, apart from the type V ones, are mixtures that contain polar molecules and ions. A sketch of the desirable technological properties of DESs is provided in Figure 1.

DES in Nanoparticle Synthesis from their Birth to 2020
The investigation of the applicability of ILs and DESs in the field of nanoparticle synthesis started with a focus on the former family, but the amount of research on DES has been growing lately. In addition, some of the features characteristic of ILs can be extended seamlessly to DESs. The most striking property of DESs in the field of nanoparticle synthesis is the high solubility of metal ion salts and complexes in several cases. As already shown by Abbott et al. [32], the solubility of some bulk metal oxides, which are almost insoluble in pure water, is greatly increased in some DESs, reaching values of up to more than 10,000 parts per million in ChCl:malonic acid 1:1 at 50 °C for Cu2O, CuO, and ZnO, and up to 90,000 ppm for ZnO in ChCl:urea 1:2 at 70 °C. In contrast, other oxides, such as iron oxides, are barely soluble in ChCl:urea 1:2. This feature can be used, for instance, to design suitable synthesis protocols based on fractional precipitation. Another key factor is the possibility of these substances acting in a dual capacity as both solvents and templates for nanostructure formation ("target solvent") [33][34][35][36][37], owing to their structural heterogeneity [38][39][40][41]. In several cases, DESs can behave as reactants as well [42][43][44].
The heterogeneity and microstructure of DESs have attracted great interest. The study by Chen et al. [45] pointed out that in "reline" (ChCl:urea 1:2), "ethaline" (ChCl:ethylene glycol 1:2), and "glyceline" (ChCl:glycerol 1:2 (the classification of this mixture as a DES or as a salt-in-solvent system has recently been debated, and the data are in favor of a 1:3 composition defining a proper DES [46])), the charged and neutral portions of the mixtures tend to separate when the liquid comes into contact with graphite

DES in Nanoparticle Synthesis from Their Birth to 2020
The investigation of the applicability of ILs and DESs in the field of nanoparticle synthesis started with a focus on the former family, but the amount of research on DES has been growing lately. In addition, some of the features characteristic of ILs can be extended seamlessly to DESs. The most striking property of DESs in the field of nanoparticle synthesis is the high solubility of metal ion salts and complexes in several cases. As already shown by Abbott et al. [32], the solubility of some bulk metal oxides, which are almost insoluble in pure water, is greatly increased in some DESs, reaching values of up to more than 10,000 parts per million in ChCl:malonic acid 1:1 at 50 • C for Cu 2 O, CuO, and ZnO, and up to 90,000 ppm for ZnO in ChCl:urea 1:2 at 70 • C. In contrast, other oxides, such as iron oxides, are barely soluble in ChCl:urea 1:2. This feature can be used, for instance, to design suitable synthesis protocols based on fractional precipitation. Another key factor is the possibility of these substances acting in a dual capacity as both solvents and templates for nanostructure formation ("target solvent") [33][34][35][36][37], owing to their structural heterogeneity [38][39][40][41]. In several cases, DESs can behave as reactants as well [42][43][44].
The heterogeneity and microstructure of DESs have attracted great interest. The study by Chen et al. [45] pointed out that in "reline" (ChCl:urea 1:2), "ethaline" (ChCl:ethylene glycol 1:2), and "glyceline" (ChCl:glycerol 1:2 (the classification of this mixture as a DES or as a salt-in-solvent system has recently been debated, and the data are in favor of a 1:3 composition defining a proper DES [46])), the charged and neutral portions of the mixtures tend to separate when the liquid comes into contact with graphite electrodes, with choline and chloride ions being attracted into the Stern layer, while the molecular components are excluded at all the potentials scanned. Similar experiments carried out using Pt (111) electrodes and the same three DESs were conducted at various potentials and at increasing water contents [47]. This study showed that the addition of water in amounts up to ≈40 wt% did not lead to the decomposition of the interfacial nanostructure, as observed in ILs even at very small water contents. Yet, the cyclic voltammetry analysis reported in the same study indicates that, at such high water concentrations, the nanostructure appears comparable to that of salt solutions. The preservation of the microscopical structure upon hydration was also demonstrated in a neutron diffraction study conducted by Hammond et al. [48], who pointed out that the microscopic features of pure reline were maintained in a water to DES molar ratio of up to 10:1 (around 42 wt% H 2 O); beyond that limit, the system can be better described as a three-component HBA:HBD:water mixture. Marked heterogeneity was evidenced as well in a molecular dynamics study conducted by Alizadeh et al. [34], who reported the fate of ethaline's polar and nonpolar molecular groups under electrostatic potential. The calculations suggest that the DES reorganizes in order to maximize the interactions between domains of the same polarity, thus inducing strong heterogeneity in the system.
The oldest syntheses reported mainly concerned the preparation of noble metal nanoparticles with a controlled shape; in most cases, these syntheses employed Abbot's DES reline [21]: catalysts containing star-like gold NPs were synthesized through the reduction of HAuCl 4 by L-ascorbic acid in DES without surfactants or seeds at room temperature ( [49], see Figure 2). The shape could be further changed (e.g., to a snowflake or nanothorn) by adjusting the water content. Other noble metal NPS were prepared by electrosynthesis methods: in this regard, DESs can be very valuable, since they possess very wide electrochemical windows just slightly bit smaller than ILs which can be effectively coupled to the large solubility of metal oxides to set up electrochemical cells for the deposition of metal nanoparticles, achieving very efficient control over the nucleation, deposition rate, and size of the crystals obtained [50]. A further very important aspect of noble metal deposition is that DES and ILs can substitute highly toxic cyanide-based electrolytes [51].
Among these examples, the preparation of concave tetrahexahedral Pt nanocrystals by electrodeposition using reline without employing surfactants, seeds, or other chemicals but with a high control of the shape and a high surface energy was reported [52]. Twodimensional superstructures of aggregated Pd nanoparticles were electrodeposited from choline chloride:urea 1:2 onto glassy carbon foil, with the absorbed species forming an anionic layer that was observed with Ultra Small X-Ray Scattering (USAXS) [53]. Platinum icosahedral nanocrystals with high-index facets and a higher electrocatalytic activity and stability were electro-synthesized in reline [54]. Further details on the role of Deep Eutectic Solvents in the synthesis of plasmonic (Au, Ag, Pt) nanoparticles can be found in the recent review of Des et al. [55], who also describe biocompatible capping strategies that make use of polysaccharides (carrageenan), resulting in highly monodisperse nanoparticles. Other non-electrochemical redox reactions were carried out using environmentally friendly routes based on reline as a solvent: CuCl nanocrystal powder, which is a very useful catalyst for organic synthesis, was obtained either through the synproportion of CuCl 2 and Cu [56] or by the reduction of CuCl 2 by ascorbic acid [57]. Additionally, spherical, magnetic nanoparticles of ferrous ferrite (Fe 3 O 4 ) were prepared at 80 • C and successfully tested for the absorption of Cu 2+ ions, proving to be superior to NPs prepared in pure water [58]. Further examples of systems prepared in reline with co-precipitation are PbS nano/micro superstructures made from lead (IV) and thioacetamide [59], mesoporous NiO [60], and some examples of iono-thermal reactions at high temperatures/pressures (nanoflower-like α-Ni(OH) 2 and NiO [61], Ni 2 P supported on amorphous/mesoporous Ni 3 (PO 4 ) 2 -Ni 2 P 2 O 7 [62], nanosized SnO crystals [63], Fe 2 O 3 nanospindles as high-capacity anode materials [64], mesoporous Co 3 O 4 sheets or nanoparticles [65], and MnCO 3 /MnOx mesocrystals [66]). An interesting example of an "antisolvent approach" is the synthesis of ZnO nanocrystals doped with Cu(II) ions, which involves adding a controlled amount of water to solutions of bulk ZnO in DES [67]. Few studies have employed DESs other than reline; some noteworthy examples utilize ethylene glycol as the HBD partner of ChCl, the latter being used to obtain nanocrystalline SnO 2 or SnO 2 /graphene nanocomposites [68], nanoporous Ag films [69], and Ni-P alloy nanoparticles [70] to deposit Ni deposits [71], Ni-Ti nanocomposite coatings [72], or Ag films [73]. In an interesting study by Mota-Morales [74], the dispersant properties of DESs during the formation of nanoparticles and other nanocomposites were exploited for the preparation of a microporous carbon nanotube-polyacrylic acid composite using a ChCl:acrylic acid mixture. The latter DES was also successfully employed as a functional monomer to create DES-levofloxacin-imprinted Pd nanoparticles for the selective removal of pollutants from wastewater [75]. Cu(II) ions, which involves adding a controlled amount of water to solutions of bulk ZnO in DES [67]. Few studies have employed DESs other than reline; some noteworthy examples utilize ethylene glycol as the HBD partner of ChCl, the latter being used to obtain nanocrystalline SnO2 or SnO2/graphene nanocomposites [68], nanoporous Ag films [69], and Ni-P alloy nanoparticles [70] to deposit Ni deposits [71], Ni-Ti nanocomposite coatings [72], or Ag films [73]. In an interesting study by Mota-Morales [74], the dispersant properties of DESs during the formation of nanoparticles and other nanocomposites were exploited for the preparation of a microporous carbon nanotube-polyacrylic acid composite using a ChCl:acrylic acid mixture. The latter DES was also successfully employed as a functional monomer to create DES-levofloxacin-imprinted Pd nanoparticles for the selective removal of pollutants from wastewater [75]. More recently, the increasing need for even greener and more biocompatible alternatives has fostered the usage of new types of environmentally benign and low-cost mixtures, mostly belonging to the NADES family (DESs of natural origin), where the precursors are obtained from renewable feedstocks. For instance, Zainal-Abidin et al. recently reported that graphene is significantly less cytotoxic when it is functionalized with ChCl:glucose/fructose/sucrose) 2:1 or, better yet, ChCl:malonic acid 1:1, with respect to pristine or oxidized graphene owing to surface modifications [76]. NADES mixtures containing glucose, fructose, and sucrose as HBD, choline chloride, and water at different molar ratios, were employed in the synthesis of MoS2 nanosheets by Mohammadpour et al. [77]. The material prepared was stable in aqueous environments, could perform as a catalyst in hydrogen evolution reactions (HERs), and could be obtained in a higher yield compared to other exfoliating agents (average of 44% vs. 20%). New mixtures created by changing the HBA or HBD started to be explored in the last part of the 2010s: an interesting example of those belonging to the second group is the synthesis of calcite nanoparticles by the reaction of CO2 with "calcoline", a DES composed of choline chloride and calcium chloride [78]. This study demonstrates that DESs can be successfully exploited in "carbon-reduction" protocols, leading to value-added products. A modification of the acceptor moiety (HBA) was used by Adhikari et al., who reported the use of halide-free DES, where the Cl-anion of reline is replaced by nitrate, for the microwave-assisted reduction of silver salts to organic-soluble oleylamine-capped Ag nanoparticles [79]. Following on from this study, Adhikari et al. later fine-tuned a silverbased DES (1:4 silver triflate:acetamide, "argentous DES") that allowed them to obtain More recently, the increasing need for even greener and more biocompatible alternatives has fostered the usage of new types of environmentally benign and low-cost mixtures, mostly belonging to the NADES family (DESs of natural origin), where the precursors are obtained from renewable feedstocks. For instance, Zainal-Abidin et al. recently reported that graphene is significantly less cytotoxic when it is functionalized with ChCl:glucose/fructose/sucrose) 2:1 or, better yet, ChCl:malonic acid 1:1, with respect to pristine or oxidized graphene owing to surface modifications [76]. NADES mixtures containing glucose, fructose, and sucrose as HBD, choline chloride, and water at different molar ratios, were employed in the synthesis of MoS 2 nanosheets by Mohammadpour et al. [77]. The material prepared was stable in aqueous environments, could perform as a catalyst in hydrogen evolution reactions (HERs), and could be obtained in a higher yield compared to other exfoliating agents (average of 44% vs. 20%). New mixtures created by changing the HBA or HBD started to be explored in the last part of the 2010s: an interesting example of those belonging to the second group is the synthesis of calcite nanoparticles by the reaction of CO 2 with "calcoline", a DES composed of choline chloride and calcium chloride [78]. This study demonstrates that DESs can be successfully exploited in "carbon-reduction" protocols, leading to value-added products. A modification of the acceptor moiety (HBA) was used by Adhikari et al., who reported the use of halide-free DES, where the Cl-anion of reline is replaced by nitrate, for the microwave-assisted reduction of silver salts to organic-soluble oleylamine-capped Ag nanoparticles [79]. Following on from this study, Adhikari et al. later fine-tuned a silver-based DES (1:4 silver triflate:acetamide, "argentous DES") that allowed them to obtain large amounts of monodispersed colloidal silver nanocrystals of high quality despite the high metal concentration, owing to the "size focusing" effect of the DES that suppressed uncontrolled nanocrystal growth [80]. More recently, these researchers exported their methodology to flow-reactor synthesis employing dimethylammonium nitrate-polyol DES media; they were able to obtain a 1000-to 4000-fold increase in throughput compared to conventional synthesis [81]. Other noteworthy examples of HBA modifications include mixtures of non-quaternary cations, such as dimethylamine, ethylamine, and trimethylamine hydrochlorides with urea, which have been successfully used to synthesize a series of silver and selenido-stannate ([NH 2 (CH 3 ) 2 ] 2 Sn 3 Se 7 ·0.5NH(CH 3 ) 2 , [NH 4 ] 2 Sn 4 Se 9 , [NH 3 C 2 H 5 ] 2 Sn 3 Se 7 , and [NH 4 ] 3 AgSn 3 Se 8 ) crystals through the solvothermal pathway. The ammonium cations originating from the original HBA as well as those resulting from the decomposition of urea have been proven to be able to act as templating agents, leading to the establishment of three-dimensional supermolecular inorganic frameworks that show the peculiar feature of thermochromism in some cases [82]. The use of ammonium cations as hydrogen bonds, though very common and convenient, is not the only option. In fact, other inorganic salts have recently been used. For example, ionic compounds belonging to the alkali halide family have been proven to form polyol-based DES mixtures (such as CsF/KF:glycerol) that have shown very high selectivities when used as reaction media for copper-catalyzed homocoupling organic reactions [83].
Returning to DESs containing molecules of natural origin, a mixture of caffeic acid with ChCl and ethyleneglycol was used to prepare moleculary imprinted hexagonal boron nitride NPs, which were successfully employed in the solid-phase extraction of flavonoids [84], while tartaric acid was used as a DES component in a recent electrodeposition preparation of a Ti/SnO 2 -Sb electrode with a high electrochemical activity [85].
In summary, the main advantages of DES that were readily highlighted shortly after their introduction as synthesis media and that were largely demonstrated during this initial time period lie in their friendliness towards ecosystems, their highly tunable physiochemical properties, and their cheap means of preparation and handling. An additional very important and profitable feature is their intrinsic microheterogeneity, with it being possible to confer specific morphologies to the obtained nanoparticles. A possible drawback of the use of DESs is their moderate viscosity, which depends on the nature of their components, with the viscosity being lower for hydrophobic DESs and larger for sugar-based NADESs. Indeed, it has been shown that the decrease in mass diffusivity caused by viscosity affects nanoparticle growth and generally leads to NPs of a larger size [86].

Research on DES Blooms: From 2020 up to Now
The number of investigations on a multifaceted topic such as DES have increased markedly in the last few years. The simple query "Deep Eutectic Solvents" in the title, abstract, and keywords on Scopus database yielded 6474 results on 17 February 2022; a more refined inquiry ("deep eutectic solvents" AND "nanoparticles") on the same day led to 343 results, 22 of which were published in the first fifty days of 2022. The full set of trends discovered is shown below (Figure 3). During the last two years, research in this field has continued in the direction of considering new eutectic mixtures that are often cheap and biocompatible. The published studies include "wet chemistry" synthesis protocols (i.e., synthetic routes not assisted by electrochemical methods or other instrumentations, such as CVD; see Table 1 for a schematic report) as well as electrochemical deposition methods, which have already been proven to be very efficient in producing several types of nanoparticles. Among all the literature, although reline still plays an important role (since it features in approximately one out of four studies (80/343) on both traditional liquid-phase syntheses and electrodeposition), the interest in new methods has grown significantly and NADESs are becoming more and more important every day. Among the newest and most interesting investigations using "traditional" ChCl:urea, the latter DES was used: in the field of metal oxides synthesis, to prepare nontoxic photoluminescent SnO nanoparticles for cell imaging [87], in the solvothermal synthesis of iron oxide from iron monitored in operando by SANS and EXAFS [88], in the synthesis of ceria nanoparticles in a continuous microreactor [89], to conjugate Fe 3 O 4 nanoparticles on graphene oxide [90], to obtain NixCo 2 -x(OH) 3 Cl nanoparticles with an optimal Ni/Co ratio suitable for use as cathodic materials [91], as a solvent and nitrogen source for preparing fluorescent carbon dots [92], and for the synthesis of titanomagnetite NPs with enzyme-like activity [93]. Finally, reline was also used very recently as a template to prepare polyacrylates/nanohydroxyapatite scaffolds and polycrystalline sub-nanometrical chalcogen nanoparticles (SeTe) with high activity towards tumor cell lines [94]. synthesis of iron oxide from iron monitored in operando by SANS and EXAFS [88], in the synthesis of ceria nanoparticles in a continuous microreactor [89], to conjugate Fe3O4 nanoparticles on graphene oxide [90], to obtain NixCo2-x(OH)3Cl nanoparticles with an optimal Ni/Co ratio suitable for use as cathodic materials [91], as a solvent and nitrogen source for preparing fluorescent carbon dots [92], and for the synthesis of titanomagnetite NPs with enzyme-like activity [93]. Finally, reline was also used very recently as a template to prepare polyacrylates/nanohydroxyapatite scaffolds and polycrystalline subnanometrical chalcogen nanoparticles (SeTe) with high activity towards tumor cell lines [94]. Regarding electrodeposition studies conducted in reline, several examples have been published in the last two years: for instance, water-soluble magnetic iron oxide nanoparticles were prepared at the anode during the electrolysis of reline using iron electrodes [95]; ruthenium nanoparticles were electrodeposited on stainless steel from a dichloride solution [96]; core-shell Pd-hydroxide NPs were obtained through the electrochemical oxidation of formic acid [97]; Zn/ZnO nanopowders were electrodeposited over Pt electrodes electrolyzing ZnCl2 solutions [98]; copper nanoparticles were obtained from CuCl2·H2O [99]. Some of the other "traditional" mixtures prepared in the first phase of DES development together with reline-namely, ethaline (choline chloride-ethylene glycol) and glyceline (choline chloride-glycerol)have found a considerable number of applications recently. Ethaline was used as a medium for the electrodeposition of Ni nanoparticles. It was, suitable for the catalysis of methanol oxidation [100]; for the synthesis of NiS2 nanospheres [101]; and, very interestingly, for the modification of Fe2O3 NPs to produce very specific electrochemical sensors-for H2O2, acetylcholine and the antibiotic dapsone [102]. Furthermore, ChCl:EG was used as a carrier and disperser for SiO2@Fe3O4 (silica-coated magnetite) ferrofluids selective for Meloxicam [103], to electrodeposit Ni-Al nanocomposite coatings from NiCl2 and aluminum dispersions [104], to synthesize platinum hollow-opened structures with enhanced performance in the electro-chemical oxidation of methanol [105], and as a solvent for assembling Ag nanoparticles onto copper substrates [106]. Glyceline was employed in the solvothermal preparation of functionalized metal-organic framework Regarding electrodeposition studies conducted in reline, several examples have been published in the last two years: for instance, water-soluble magnetic iron oxide nanoparticles were prepared at the anode during the electrolysis of reline using iron electrodes [95]; ruthenium nanoparticles were electrodeposited on stainless steel from a dichloride solution [96]; core-shell Pd-hydroxide NPs were obtained through the electrochemical oxidation of formic acid [97]; Zn/ZnO nanopowders were electrodeposited over Pt electrodes electrolyzing ZnCl 2 solutions [98]; copper nanoparticles were obtained from CuCl 2 ·H 2 O [99]. Some of the other "traditional" mixtures prepared in the first phase of DES development together with reline-namely, ethaline (choline chloride-ethylene glycol) and glyceline (choline chloride-glycerol)-have found a considerable number of applications recently. Ethaline was used as a medium for the electrodeposition of Ni nanoparticles. It was, suitable for the catalysis of methanol oxidation [100]; for the synthesis of NiS 2 nanospheres [101]; and, very interestingly, for the modification of Fe 2 O 3 NPs to produce very specific electrochemical sensors-for H 2 O 2 , acetylcholine and the antibiotic dapsone [102]. Furthermore, ChCl:EG was used as a carrier and disperser for SiO 2 @Fe 3 O 4 (silica-coated magnetite) ferrofluids selective for Meloxicam [103], to electrodeposit Ni-Al nanocomposite coatings from NiCl 2 and aluminum dispersions [104], to synthesize platinum hollow-opened structures with enhanced performance in the electro-chemical oxidation of methanol [105], and as a solvent for assembling Ag nanoparticles onto copper substrates [106]. Glyceline was employed in the solvothermal preparation of functionalized metal-organic framework (MOF) nanoparticles containing zirconium [107], to immobilize Pd nanoparticles [108], and to deposit ZnO in situ on graphene sheets [109]. However, the real novelty of the last period consisted, as stated above, in the very large increase in the use of many new and alternative mixtures, often including biomolecules of natural origin. For instance, the excellent capabilities of glycerol as hydrogen bond donor in DES were further enhanced by the addition of malic acid and D-fructose in a 1:1:1: mole ratio (MaFruGly). MaFruGly was used to disperse Al 2 O 3 into a nanofluid that is capable of extracting polyphenols and other bioactive compounds from olive oil pomaces and leaves [110]. Other examples of such biocompatible mixtures include choline chloride:glucose, which was used to prepare sodium hyaluronate/dopamine/AgNPs hydrogels [111]; ChCl:xylitol, which was employed to modify magnetic titania NPs with Fe 3 O 4 @TiO 2 @DES [112]; and choline chloride:gluconic acid DES, which was used to prepare a cobalt-DES precursor that was finally pyrolyzed into Co nanoparticles supported on nitrogen-doped porous carbon (Co@NPC). The latter acts as a bifunctional catalyst for water splitting (H 2 production) and glucose oxidation (GOR) in an electro-chemical cell [113]. Along the same line, carbon-doped copper oxide catalysts with a high selectivity in CO 2 electrochemical reduction were produced by the calcination of sugar-urea DES (glucose:urea and galactose:urea) containing copper salts [114]. Mixtures containing carboxylic acids have been described in several examples: ChCl + oxalic acid and malonic acid, together with urea, fructose, and ethylene glycol, were used to synthesize MgFe 2 O 4 nanoparticles with a high sensitivity and selectivity towards nitrofenantoine and 4-nitrophenol [115]. Pd nanoparticles confined in nanocellulose with a high catalytic chemoselectivity and activity were prepared from choline chloride and oxalic acid dihydrate 1:1 [116] (this mixture was also employed as a medium to synthesize porous Fe 3 O 4 nanosheets with high electrocatalytic performances starting from commercial powders) [117]. An example of a mixture of choline and inorganic salts is choline:Na 2 SO 3 2:1, a "reductant" solvent where sulfur-functionalized graphene oxide NPs for Li-S batteries were synthesized using a chemical reduction/co-precipitation method [118].
A relevant portion of the recent studies on this topic has focused on magnetic nanoparticles containing Fe 3 O 4 (or Fe 2 O 3 ) and organic moieties or enzymes, which could be assembled in a few examples of DESs: acrylic acid-Fe 3 O 4 composites were obtained from acrylic acid:menthol-type V DES used in the detection of pesticides [119], whereas macroporous polyacrylamide γ-maghemite composites were prepared in acetic acid:menthol [120]. Nano-Fe 3 O 4 was prepared in NADES betaine-urea, coated with silicon, and successfully employed to immobilize β-glucosidase [121]. magnetite nanocubes with anticancer and photo-Fenton efficacy were synthesized in ChCl:citric acid by Sakthi Sri et al. [122]; poly glycerol@Fe 3 O 4 nanoparticles (as HBD) were treated with choline chloride, giving a branched poly (DES)@ Fe 3 O 4 fluid that was used as draw solute in forward osmosis [123], whereas DES coupled to Fe 3 O 4 -MUiO-66-NH 2 (a metal organic framework composed of zirconia clusters cross-linked by terephtalic acid) obtained from mixtures of quaternary ammonium salts different from choline, such as benzyltributylammonium chloride (BTBAC), benzyltributylammonium bromide (BTBAB), tetrabutylammonium chloride (TBAC) as HBA, and lactic or glycolic acid such as HBD was employed to adsorb pharmaceuticals and personal care products (PPCPs). The magnetic nanoparticles could be easily separated and recovered from the adsorbed species using a magnet [124]. Other examples of quaternary ammonium salts include TBAB (tetrabutylammonium bromide), which was combined with imidazole in a DES. The latter was employed as a solvent to immobilize Pd nanoparticles onto a covalent organic framework, finally resulting in a heterogeneous catalyst used for the phosphorylation of aryl bromides [125]. Furthermore, CTAB (cetyltrimethylammonium bromide), which combines with acetic acid in a 1:1 mass ratio to create a liquid mixture, was used for the formation of ceria nanoparticles with remarkable photocatalytic activity by Iqbal and coworkers [126,127]. Other sugar-based DESs similar to those cited above-namely, dl-menthol:oleyl alcohol 1:1.2-were employed to prepare an NDDES (nano dispersed DES) mixture containing boron nitride nanoparticles, with excellent properties as a heat-transfer nanofluid [128]. A comprehensive survey on the use of DES as a base fluid for heat-transfer nanofluids can be found in [29].

Lewis Acid DES (LADES)
A smaller number of studies were dedicated to DES without quaternary ammonium salts, containing metal salts (often hydrated) such as HBA and hydrogen bond donors such as urea or acetamide. This family of DES is known as LADES (Lewis Acid DES)) [129], compared to the more common "BADES" (with Brønsted acids, such as choline chloride + oxalic acid). According to the Abbot classification, LADES belong to Type I, II, or IV DES (such as, for instance, ChCl:2ZnCl 2 , ChCl:2CrCl 3 ·6H 2 O, ZnCl 2 :urea 1:3.5 (or:4) melts), as do several amide-nitrate eutectics [130] (such as LiNO 3 :acetamide 22:78 eutectic, which was recently described as a valuable medium for electrochemical capacitors [131]) and the DES mixture already described (silver triflate:acetamide [79]), while Type III DES can form only BADES. The existence of these non-conventional melts was quite recently discussed regarding the preparation or modification of inorganic nanoparticles. These DES include chloride salts, which have been employed in three different preparations of titania-based nanomaterials: the nano-photocatalyst n-TiO 2 -P25@TDI@DES, which is highly recyclable and selective, was obtained by combining TiO 2 -P25 powder (70% anatase, 30% rutile) with a ZnCl 2 :urea 1:4 mixture using 2,4-toluene diisocyanate (TDI) as a bifunctional covalent linker. The nanocatalyst was employed successfully in the oxidation of benzyl alcohols to aldehydes and sulfides to sulfoxides [132,133]; the synergy between LADES and NPs was also exploited in the coupling between "Hierarchical TiO 2 " (H-TiO 2 ) microspheres and FeCl 2 /CuCl 2 urea in 1:4 mixtures to increase the reaction yields in the preparation of pyrrolidyn-2-one heterocycles [134] and by grafting the ZnCl 2 :urea 1:4 mixture onto magnetic ferrite nanoparticles to generate a DES@MNP homogeneous catalyst (which was found to be "magnetically recyclable" at the end of one-pot multicomponent syntheses [135]). Coming back to the synthesis of the nanoparticles themselves, some lanthanide-based type IV DES (Ln-DES) containing hydrated nitrates were prepared [136]. These mixtures show unusually low viscosity and surface tensions and the presence of fluxional oligomeric polyanions and polycations, and were employed as reaction media in the combustion synthesis of oxides; more recently, actinide-based type IV DES (An-DES) were obtained by mixing uranyl nitrate hexahydrate UO 2 (NO 3 ) 2 ·6H 2 O (UNH) with urea in different ratios (Figure 4), finding 0.2:0.8 to be the optimal UNH:urea mole fraction, with a quite low eutectic temperature of −5.2 • C. This liquid was employed to prepare UO 2 nanoparticles through an optimized electrosynthesis path [137]. Some examples of reactions in LADES are given in Table 2. and the presence of fluxional oligomeric polyanions and polycations, and were employed as reaction media in the combustion synthesis of oxides; more recently, actinide-based type IV DES (An-DES) were obtained by mixing uranyl nitrate hexahydrate UO2(NO3)2·6H2O (UNH) with urea in different ratios (Figure 4), finding 0.2:0.8 to be the optimal UNH:urea mole fraction, with a quite low eutectic temperature of −5.2 °C. This liquid was employed to prepare UO2 nanoparticles through an optimized electrosynthesis path [137]. Some examples of reactions in LADES are given in Table 2.  [138]; choline chloride with ethanolamine or polyvinyl alcohol [139,140]; and choline chloride coupled with carboxylic acids (such as oxalic or lactic acid [141]) or with inorganic salts (Gly-K2CO3) [142]), DES lactic acid-betaine [142], and menthol-based melts (e.g., menthol:dodecanoic acid [143]). Aside from metal nanoparticles, DES are finding wide application nowadays in the production of lignin and cellulose nanoparticles. A basic knowledge of this widely investigated topic, though not closely related to the focus of this article, can help in showing further examples of eutectic mixtures, particularly the newest natural biocompatible ones, that could somehow be adapted and employed for the synthesis of systems containing metals. Among the most recent examples worth mentioning are mixtures of choline chloride:glycerol (or ethylene glycol) with AlCl 3 [138]; choline chloride with ethanolamine or polyvinyl alcohol [139,140]; and choline chloride coupled with carboxylic acids (such as oxalic or lactic acid [141]) or with inorganic salts (Gly-K 2 CO 3 ) [142]), DES lactic acid-betaine [142], and menthol-based melts (e.g., menthol:dodecanoic acid [143]).

A Prototypical Synthesis
In order to show the potential and ease of obtaining inorganic nanoparticles in DES, we show a prototypical NP synthesis carried out in DES in the following paragraph. In particular, the co-precipitation of the mixed salt Fe 3 O 4 (structurally FeO·Fe 2 O 3 ) from Fe 2+ and Fe 3+ soluble salt solutions in Choline-Urea 1:2 DES (reline) upon the addition of sodium hydroxide will be shown. The procedure was first reported in [56] and was modified for this test preparation according to the following protocol: (a) Preparation of DES Totals of 11.108 g of dry choline chloride (MM = 139.62, 80 mmoles) and 9.610 g of urea (MM = 60.06, 160 mmoles) were weighted separately and kept in closed containers. The two solids were then mixed in a sealable vial at room temperature. Quite rapidly, the two solids when put in contact formed a sluggish agglomerate that became more fluid and transparent with gentle heating (35-40 • C); see Figure 3, first panel.
(b) Preparation of the solution Totals of 0.130 g of FeCl 3 (0.8 mmoles) and 0.167 g of FeSO 4 ·7 H 2 O (0.6 mmol) were weighed and added to 1.559 g of the prepared DES in a 25 mL beaker. The dissolution was accelerated by heating the mixture at 80 • C, resulting in an orange transparent liquid; see Figure 5, second panel. The total amount of water introduced into the system (by counting the hydration water molecules coming from FeSO 4 and estimating those coming from the average absorbed water content of the two DES precursors (ChCl and urea) by weighing samples of the powders before and after a three day-long drying treatment at 50 • C in an oven) was well below the upper limit (10 moles of water per mole of DES), as identified in the neutron diffraction study by Hammond et al. [48], beyond which the microscopic features of pure reline were lost and the system turned into a three-component HBA:HBD:water mixture.

(c) Precipitation
A total of 0.187 g of NaOH (previously powdered in an agate mortar, 46.7 mmol) was added to the solution at 80 °C under magnetic stirring (600 rpm). After 20 min, a black precipitate formed; see Figure 5, third panel. The precipitate was washed with 20 mL of distilled water four times and centrifuged for 5 min at 3000 rpm after each rinse cycle. The excess of DES crystallized upon contact with cold water but was gradually solubilized. The final pH after the washing was around 7, signaling that the excess amounts of NaOH and urea had been washed out.
(d) Drying The washed precipitate was collected from the vial, dried at 40 °C and finally rolled into a bead. The bead was put into an Eppendorf tube, and its ferromagnetism was qualitatively tested with a magnetic stir bar ( Figure 5, fourth panel)

Conclusions
In this small contribution, an overview of the newest and most important features of Deep Eutectic Solvents in the field of nanoparticle synthesis is given. We demonstrate that these mostly benign and inexpensive reaction media can be employed in different types of wet synthesis, as well as in electrochemical preparations. The reported reaction schemes

(c) Precipitation
A total of 0.187 g of NaOH (previously powdered in an agate mortar, 46.7 mmol) was added to the solution at 80 • C under magnetic stirring (600 rpm). After 20 min, a black precipitate formed; see Figure 5, third panel. The precipitate was washed with 20 mL of distilled water four times and centrifuged for 5 min at 3000 rpm after each rinse cycle. The excess of DES crystallized upon contact with cold water but was gradually solubilized. The final pH after the washing was around 7, signaling that the excess amounts of NaOH and urea had been washed out.
(d) Drying The washed precipitate was collected from the vial, dried at 40 • C and finally rolled into a bead. The bead was put into an Eppendorf tube, and its ferromagnetism was qualitatively tested with a magnetic stir bar ( Figure 5, fourth panel)

Conclusions
In this small contribution, an overview of the newest and most important features of Deep Eutectic Solvents in the field of nanoparticle synthesis is given. We demonstrate that these mostly benign and inexpensive reaction media can be employed in different types of wet synthesis, as well as in electrochemical preparations. The reported reaction schemes are often straightforward and do not require complicated set-ups or equipment. The inherent inhomogeneity of the liquid mixtures exerts a direct templating effect without the use of any additives, and nanosystems of different topologies/shapes can be obtained. This field is being actively developed, as seen by the ever-increasing number of articles published, and its huge potential will surely continue to be explored, in search of new materials with beneficial technological properties.